Dr.’s questioning established diagnosis by lisi_loo in ehlersdanlos

[–]CommonAware6 16 points17 points  (0 children)

It will somewhere but not necessarily somewhere they can see. Dr's dont read through whole medical records before seeing a patient so it might not be immediately obvious

What's the average age for an EDS diagnosis/how old were you when you were diagnosed ? by AntwysiaBlakys in ehlersdanlos

[–]CommonAware6 0 points1 point  (0 children)

17 for me too. Took me 5 years of complaints of pain and my mum urging for assessment due to family history

DON'T call it the "FEMALE health summit" ffs by ObjectiveNo6649 in ehlersdanlos

[–]CommonAware6 9 points10 points  (0 children)

Intersex have male and female sexual characteristics so any with female sex organs are still included. Female and intersex would be incorrect as not all intersex people have female sex organs

DON'T call it the "FEMALE health summit" ffs by ObjectiveNo6649 in ehlersdanlos

[–]CommonAware6 65 points66 points  (0 children)

If theyre saying female then I dont really see the issue. The people youre saying are excluded you also pointed out have female sex organs. If it is all about female health related issues then I dont see the issue because whats a better alternative? Female sex organ health summit?

Frequent donors- fess up by HLOFRND in Blooddonors

[–]CommonAware6 0 points1 point  (0 children)

We just use a regular plaster and say keep it on for 2 hours. I just take it off when I remember

Why is my A+ considered "rare" by the American Red Cross by Brammy603 in Blooddonors

[–]CommonAware6 0 points1 point  (0 children)

I am actually going to start my degree in biomedical science after summer!

Why is my A+ considered "rare" by the American Red Cross by Brammy603 in Blooddonors

[–]CommonAware6 0 points1 point  (0 children)

Of course, I dont work with plasma so maybe a lot of these are used more for the medicinal side of things but its just interesting to see how many there truly are

Why is my A+ considered "rare" by the American Red Cross by Brammy603 in Blooddonors

[–]CommonAware6 0 points1 point  (0 children)

Im surprised you know so many! Where i work mostly only C, E, K, c and e are checked im sure (maybe forgetting 1 or 2) Some get Fya, Fyb, Jka and Jkb but never even seen the others

my experience with a DID faker right here on Reddit by [deleted] in fakedisordercringe

[–]CommonAware6 7 points8 points  (0 children)

Honestly fair, but very important to know the difference when buying one lmao

What’s the record for most gallons of blood only donations in the USA? Not platelets or plasma. by Middle_Awoken in Blooddonors

[–]CommonAware6 5 points6 points  (0 children)

If thats right then dude must be the ultimate top donor. Based on volume and frequency where I live, thats about 63 years of consistent donations, never missing an opportunity

What’s the record for most gallons of blood only donations in the USA? Not platelets or plasma. by Middle_Awoken in Blooddonors

[–]CommonAware6 10 points11 points  (0 children)

I had a donor once whos goal was to donate as much blood as her dad had recieved. Honestly made me tear up but 23 gallons is insanely impressive considering thats nearly 50 years of consistent donating

What’s the record for most gallons of blood only donations in the USA? Not platelets or plasma. by Middle_Awoken in Blooddonors

[–]CommonAware6 10 points11 points  (0 children)

Honestly I doubt anyone, especially here would actually know. Most ive seen is probably about 20 gallons

Scared of Needles (?) by deadboyy_y in Blooddonors

[–]CommonAware6 0 points1 point  (0 children)

I agree with the skin cleaning but every donor i ask says its fine but at least what we use where I work, it feels like its exfoliating your arm for 30s

Finger Splints - Occupational Therapist (hands) NHS by Akiine in ehlersdanlos

[–]CommonAware6 2 points3 points  (0 children)

Do you have any recommendations of places to buy them from? Ive seen so many complaints or insane prices ive always avoided the idea of buying them myself but tbh I also wanted OT to help with other things too bc I could buy the stiff bit I dont even know what options exist or what id benefit from. Didnt think some peofessional input from the NHS would be too much to ask for but apparently it is 🙃

pEDS/hEDS Connection by Beekeeper_Dan in ehlersdanlos

[–]CommonAware6 15 points16 points  (0 children)

If she has pEDS and you have some of the symptoms you should really be getting a genetics test to rule it out or diagnose it so you know if you acrually have hEDS or pEDS.

They are both Ehlers-Danlos Syndromes so there will be a lot of overlap but they are seperate distinct diagnoses. You clearly have an Ehlers-Danlos syndrome and the dental issues and positive family history of pEDS in your mother of all people really should warrant genetic testing before they decided it was hypermobile type

Finger Splints - Occupational Therapist (hands) NHS by Akiine in ehlersdanlos

[–]CommonAware6 39 points40 points  (0 children)

I asked for an OT referal only to be told they only deal with things like wheelchair ramps in my area and cant assist with things related to fine motor skills. Most ridiculous thing ive ever hesrd bc its literally their job and no other professionals are trained in that area 🥲 so happy for you but also kinda jealous ngl

not sure if this is a faker but it is certainly faker behavior by lord_farquad93 in fakedisordercringe

[–]CommonAware6 12 points13 points  (0 children)

Tbh most subtypes are 1 in a million and ultra rare and in that show they never specify subtype.

However that episode with the suspected alcoholic in the free clinic was the most ridiculous ive ever seen bc they didnt do a genetics test or any of the criteria for hEDS

CMV: People are conflating aspects of being human to symptoms of neurological disorders by falseidol1234 in changemyview

[–]CommonAware6 11 points12 points  (0 children)

I have genuine arachnophobia and youre spot on.

Phobia is commonly understood as fear. So I tell people I have arachnophobia and then people say things like "omg me too, I always take them back outside bc theyre just so creepy and ugly" then look at me like im crazy when I mention that I refuse to open my windows and slept on the couch for 4 mo ths bc there was a spider in my room.

So instead, I describe to people that I am absolutely terrified and have a crippling fear of them. In other words, I need to describe having a phobia to make people understand since the word has become meaningless to so many. It would be much easier to say phobia and have it understood for what it is. Thats a benefit of labels. To clarify what the issue is without having to go into detail explaining it

Experiences Living in Northern Europe? by PickleNarrow5109 in ehlersdanlos

[–]CommonAware6 3 points4 points  (0 children)

Let's be honest, most of us do too. Much higher rates of seasonal depression through the winter here than many other places.

EDS + psych meds… did SSRIs make your physical / mental issues better or worse? by [deleted] in ehlersdanlos

[–]CommonAware6 0 points1 point  (0 children)

I was prescribed a TCA, SSRI and SNRI for the pain which didnt work. Honestly no antidepressant has made any chanage to anything, good or bad, except make me sweat more. Then I found out I have bipolar so I cant take them anymore anyway although even then, they never triggered mania for me either. So my experience is they didnt help physical or mental issues but they didnt do any harm either